deltatrials
Completed PHASE2 INTERVENTIONAL 2-arm NCT00457639

Cholic Acid for Hepatic Steatosis in Lipodystrophy

Phase II Study of Cholic Acid for Hepatic Steatosis in Lipodystrophy Patients

Sponsor: FDA Office of Orphan Products Development

Interventions Cholic Acid
Updated 8 times since 2017 Last updated: Aug 4, 2025 Started: Apr 30, 2006 Primary completion: Apr 30, 2011 Completion: Apr 30, 2011
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A PHASE2 clinical study on Hepatic Steatosis, this trial is completed. The trial is conducted by FDA Office of Orphan Products Development and has accumulated 8 data snapshots since 2006. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

~Jan 2017 – ~Feb 2017 · 31 days · monthly snapshotUnknown Status~Feb 2017 – ~Jun 2018 · 16 months · monthly snapshotUnknown Status~Jun 2018 – ~Feb 2019 · 8 months · monthly snapshotUnknown Status~Feb 2019 – ~Jan 2021 · 23 months · monthly snapshotCompleted~Jan 2021 – ~Jul 2024 · 42 months · monthly snapshotCompleted~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotCompleted~Sep 2024 – ~Sep 2025 · 12 months · monthly snapshotCompleted~Sep 2025 – present · 11 months · monthly snapshotCompleted

Change History

8 versions recorded
  1. Sep 2025 — Present [monthly]

    Completed PHASE2

  2. Sep 2024 — Sep 2025 [monthly]

    Completed PHASE2

  3. Jul 2024 — Sep 2024 [monthly]

    Completed PHASE2

  4. Jan 2021 — Jul 2024 [monthly]

    Completed PHASE2

  5. Feb 2019 — Jan 2021 [monthly]

    Completed PHASE2

    Status: Unknown StatusCompleted

Show 3 earlier versions
  1. Jun 2018 — Feb 2019 [monthly]

    Unknown Status PHASE2

  2. Feb 2017 — Jun 2018 [monthly]

    Unknown Status PHASE2

  3. Jan 2017 — Feb 2017 [monthly]

    Unknown Status PHASE2

    First recorded

Apr 2006

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • FDA Office of Orphan Products Development
  • University of Texas Southwestern Medical Center
Data source: University of Texas Southwestern Medical Center

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations